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Ophthalmic Genetics|June 23, 2022
A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese familyVanita Berry, Kaoru Fujinami, Kiyofumi Mochizuki, et al.
Journal of Vision|August 7, 2014
What monitor can replace the cathode-ray tube for visual stimulation to elicit multifocal electroretinograms?Celso Soiti Matsumoto, Kei Shinoda, Harue Matsumoto, et al.
Journal of Vision|September 7, 2014
Binocular interaction of visually evoked cortical potentials elicited by dichoptic binocular stimulationCelso Soiti Matsumoto, Ryota Nakagomi, Harue Matsumoto, et al.
Japanese Journal of Ophthalmology|July 3, 2017
Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophyTakaaki Hayashi, Hiroyuki Sasano, Satoshi Katagiri, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 22, 2014
Autosomal recessive cone-rod dystrophy associated with compound heterozygous mutations in the EYS geneSatoshi Katagiri, Masakazu Akahori, Takaaki Hayashi, et al.
Ophthalmic Genetics|August 13, 2014
Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High MyopiaSatoshi Katagiri, Takaaki Hayashi, Kazutoshi Yoshitake, et al.
Investigative Ophthalmology & Visual Science|December 3, 2017
Parafoveal Photoreceptor Abnormalities in Asymptomatic Patients With RP1L1 Mutations in Families With Occult Macular DystrophyYu Kato, Gen Hanazono, Kaoru Fujinami, et al.
Japanese Journal of Ophthalmology|August 15, 2016
New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndromeKazuki Kuniyoshi, Takaaki Hayashi, Hiroyuki Sakuramoto, et al.
Experimental Animals|May 21, 2010
Comparative proteomic analyses of macular and peripheral retina of cynomolgus monkeys (Macaca fascicularis)Haru Okamoto, Shinsuke Umeda, Takehiro Nozawa, et al.
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